260 related articles for article (PubMed ID: 31836699)
1. NBS1 interacts with HP1 to ensure genome integrity.
Bosso G; Cipressa F; Moroni ML; Pennisi R; Albanesi J; Brandi V; Cugusi S; Renda F; Ciapponi L; Polticelli F; Antoccia A; di Masi A; Cenci G
Cell Death Dis; 2019 Dec; 10(12):951. PubMed ID: 31836699
[TBL] [Abstract][Full Text] [Related]
2. The Drosophila Nbs protein functions in multiple pathways for the maintenance of genome stability.
Ciapponi L; Cenci G; Gatti M
Genetics; 2006 Jul; 173(3):1447-54. PubMed ID: 16648644
[TBL] [Abstract][Full Text] [Related]
3. The Drosophila Mre11/Rad50 complex is required to prevent both telomeric fusion and chromosome breakage.
Ciapponi L; Cenci G; Ducau J; Flores C; Johnson-Schlitz D; Gorski MM; Engels WR; Gatti M
Curr Biol; 2004 Aug; 14(15):1360-6. PubMed ID: 15296753
[TBL] [Abstract][Full Text] [Related]
4. Regulation of Mre11/Rad50 by Nbs1: effects on nucleotide-dependent DNA binding and association with ataxia-telangiectasia-like disorder mutant complexes.
Lee JH; Ghirlando R; Bhaskara V; Hoffmeyer MR; Gu J; Paull TT
J Biol Chem; 2003 Nov; 278(46):45171-81. PubMed ID: 12966088
[TBL] [Abstract][Full Text] [Related]
5. Telomere instability in a human tumor cell line expressing NBS1 with mutations at sites phosphorylated by ATM.
Bai Y; Murnane JP
Mol Cancer Res; 2003 Dec; 1(14):1058-69. PubMed ID: 14707289
[TBL] [Abstract][Full Text] [Related]
6. Molecular characterization of the Schizosaccharomyces pombe nbs1+ gene involved in DNA repair and telomere maintenance.
Ueno M; Nakazaki T; Akamatsu Y; Watanabe K; Tomita K; Lindsay HD; Shinagawa H; Iwasaki H
Mol Cell Biol; 2003 Sep; 23(18):6553-63. PubMed ID: 12944481
[TBL] [Abstract][Full Text] [Related]
7. Mre11-Rad50-Nbs complex is required to cap telomeres during Drosophila embryogenesis.
Gao G; Bi X; Chen J; Srikanta D; Rong YS
Proc Natl Acad Sci U S A; 2009 Jun; 106(26):10728-33. PubMed ID: 19520832
[TBL] [Abstract][Full Text] [Related]
8. Cleavage of the BRCT tandem domains of nibrin by the 657del5 mutation affects the DNA damage response less than the Arg215Trp mutation.
Mendez G; Cilli D; Berardinelli F; Viganotti M; Ascenzi P; Tanzarella C; Antoccia A; di Masi A
IUBMB Life; 2012 Oct; 64(10):853-61. PubMed ID: 22941933
[TBL] [Abstract][Full Text] [Related]
9. A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling "Nijmegen breakage syndrome" phenotype.
Berardinelli F; di Masi A; Salvatore M; Banerjee S; Myung K; De Villartay JP; Revy P; Plebani A; Soresina A; Taruscio D; Tanzarella C; Antoccia A
Eur J Med Genet; 2007; 50(3):176-87. PubMed ID: 17395558
[TBL] [Abstract][Full Text] [Related]
10. Ataxia-telangiectasia-like disorder (ATLD)-its clinical presentation and molecular basis.
Taylor AM; Groom A; Byrd PJ
DNA Repair (Amst); 2004; 3(8-9):1219-25. PubMed ID: 15279810
[TBL] [Abstract][Full Text] [Related]
11. The fission yeast Rad32 (Mre11)-Rad50-Nbs1 complex is required for the S-phase DNA damage checkpoint.
Chahwan C; Nakamura TM; Sivakumar S; Russell P; Rhind N
Mol Cell Biol; 2003 Sep; 23(18):6564-73. PubMed ID: 12944482
[TBL] [Abstract][Full Text] [Related]
12. The importance of making ends meet: mutations in genes and altered expression of proteins of the MRN complex and cancer.
Dzikiewicz-Krawczyk A
Mutat Res; 2008; 659(3):262-73. PubMed ID: 18606567
[TBL] [Abstract][Full Text] [Related]
13. NBS1 deficiency promotes genome instability by affecting DNA damage signaling pathway and impairing telomere integrity.
Hou YY; Toh MT; Wang X
Cell Biochem Funct; 2012 Apr; 30(3):233-42. PubMed ID: 22161642
[TBL] [Abstract][Full Text] [Related]
14. Identification of the interactors of human nibrin (NBN) and of its 26 kDa and 70 kDa fragments arising from the NBN 657del5 founder mutation.
Cilli D; Mirasole C; Pennisi R; Pallotta V; D'Alessandro A; Antoccia A; Zolla L; Ascenzi P; di Masi A
PLoS One; 2014; 9(12):e114651. PubMed ID: 25485873
[TBL] [Abstract][Full Text] [Related]
15. Chromosomal Instability and Molecular Defects in Induced Pluripotent Stem Cells from Nijmegen Breakage Syndrome Patients.
Halevy T; Akov S; Bohndorf M; Mlody B; Adjaye J; Benvenisty N; Goldberg M
Cell Rep; 2016 Aug; 16(9):2499-511. PubMed ID: 27545893
[TBL] [Abstract][Full Text] [Related]
16. Retroviral expression of the NBS1 gene in cultured Nijmegen breakage syndrome cells restores normal radiation sensitivity and nuclear focus formation.
Cerosaletti KM; Desai-Mehta A; Yeo TC; Kraakman-Van Der Zwet M; Zdzienicka MZ; Concannon P
Mutagenesis; 2000 May; 15(3):281-6. PubMed ID: 10792024
[TBL] [Abstract][Full Text] [Related]
17. Genomic instability, endoreduplication, and diminished Ig class-switch recombination in B cells lacking Nbs1.
Reina-San-Martin B; Nussenzweig MC; Nussenzweig A; Difilippantonio S
Proc Natl Acad Sci U S A; 2005 Feb; 102(5):1590-5. PubMed ID: 15668392
[TBL] [Abstract][Full Text] [Related]
18. Importin KPNA2 is required for proper nuclear localization and multiple functions of NBS1.
Tseng SF; Chang CY; Wu KJ; Teng SC
J Biol Chem; 2005 Nov; 280(47):39594-600. PubMed ID: 16188882
[TBL] [Abstract][Full Text] [Related]
19. Nijmegen breakage syndrome and functions of the responsible protein, NBS1.
Antoccia A; Kobayashi J; Tauchi H; Matsuura S; Komatsu K
Genome Dyn; 2006; 1():191-205. PubMed ID: 18724061
[TBL] [Abstract][Full Text] [Related]
20. SV40 T antigen interacts with Nbs1 to disrupt DNA replication control.
Wu X; Avni D; Chiba T; Yan F; Zhao Q; Lin Y; Heng H; Livingston D
Genes Dev; 2004 Jun; 18(11):1305-16. PubMed ID: 15175262
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
